Durable polymer-aerogel based superhydrophobic coatings: a composite material

ABSTRACT

Provided are polymer-aerogel composite coatings, devices and articles including polymer-aerogel composite coatings, and methods for preparing the polymer-aerogel composite. The exemplary article can include a surface, wherein the surface includes at least one region and a polymer-aerogel composite coating disposed over the at least one region, wherein the polymer-aerogel composite coating has a water contact angle of at least about 140° and a contact angle hysteresis of less than about 1°. The polymer-aerogel composite coating can include a polymer and an ultra high water content catalyzed polysilicate aerogel, the polysilicate aerogel including a three dimensional network of silica particles having surface functional groups derivatized with a silylating agent and a plurality of pores.

RELATED APPLICATIONS

This application is a divisional application of U.S. patent applicationSer. No. 13/121,150 filed May 4, 2011 (now allowed), which is a U.S.National Stage Application of PCT/US2009/049205 filed Jun. 30, 2009which claims priority from U.S. Provisional Patent Application Ser. No.61/077,143, filed Jun. 30, 2008, which is hereby incorporated byreference in its entirety.

GOVERNMENT RIGHTS

This invention was made with government support under Contract Nos.DE-AC04-94AL85000 between Sandia Corporation and the U.S. Department ofEnergy and FA9550-06-C-0033 awarded by the U.S. Air Force Office ofScientific Research. The U.S. Government has certain rights in thisinvention.

FIELD OF THE INVENTION

The subject matter of this invention relates to protective coatings and,more particularly, to polymer-aerogel composites.

BACKGROUND OF THE INVENTION

Aerogels are unique solids with up to 99% porosity. Such largeporosities confer a number of useful properties to aerogels, includinghigh surface area, low refractive index, low dielectric constant, lowthermal-loss coefficient, and low sound velocity. However, the potentialof aerogels has not generally been realized because conventionalsupercritical aerogel processing is energy intensive and conventionalareogels lack durability. Furthermore, most superhydrophobic coatingscontain fluorine which can be environmentally unfriendly and may not becost effective to manufacture.

Thus, there is a need to overcome these and other problems of the priorart and to provide durable and inexpensive superhydrophobicpolymer-aerogel coating.

SUMMARY OF THE INVENTION

According to various embodiments, there is a method for preparing apolymer-aerogel composite coating. The method can include providing asuperhydrophobic coating solution, the superhydrophobic coating solutionincluding a surface derivatized polysilicate aerogel dispersed in afirst solvent, the polysilicate aerogel including a three dimensionalnetwork of silica particles having surface functional groups derivatizedwith a silylating agent. The method can also include adding a polymersolution to the superhydrophobic coating solution to form apolymer-aerogel blend solution, wherein the polymer solution can includeone or more polymers dispersed in a second solvent and dissolving thepolymer in the polymer-aerogel blend solution at a first temperature.The method can further forming a polymer-aerogel composite coating byapplying the polymer-aerogel blend solution to a substrate surface whilekeeping the polymer-aerogel blend solution at the first temperature,such that the polymer wets the aerogel in the polymer-aerogel compositecoating.

In accordance with various embodiments, there is an article including asurface, wherein the surface comprises at least one region and apolymer-aerogel composite coating disposed over the at least one region,wherein the polymer-aerogel composite coating can include a polymer andan ultra high water content catalyzed polysilicate aerogel, thepolysilicate aerogel including a three dimensional network of silicaparticles having surface functional groups derivatized with a silylatingagent and a plurality of pores, wherein the polymer-aerogel compositecoating has a water contact angle of at least about 140° and a contactangle hysteresis of less than about 1°.

Additional advantages of the embodiments will be set forth in part inthe description which follows, and in part will be obvious from thedescription, or may be learned by practice of the invention. Theadvantages will be realized and attained by means of the elements andcombinations particularly pointed out in the appended claims.

It is to be understood that both the foregoing general description andthe following detailed description are exemplary and explanatory onlyand are not restrictive of the invention, as claimed.

The accompanying drawings, which are incorporated in and constitute apart of this specification, illustrate embodiments of the invention andtogether with the description, serve to explain the principles of theinvention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a method for preparing a polymer-aerogel composite coatingin accordance with the present teachings.

FIG. 2 schematically illustrates a cross section of a portion of anexemplary article in accordance with the present teachings.

DESCRIPTION OF THE EMBODIMENTS

Reference will now be made in detail to the present embodiments,examples of which are illustrated in the accompanying drawings. Whereverpossible, the same reference numbers will be used throughout thedrawings to refer to the same or like parts.

Notwithstanding that the numerical ranges and parameters setting forththe broad scope of the invention are approximations, the numericalvalues set forth in the specific examples are reported as precisely aspossible. Any numerical value, however, inherently contains certainerrors necessarily resulting from the standard deviation found in theirrespective testing measurements. Moreover, all ranges disclosed hereinare to be understood to encompass any and all sub-ranges subsumedtherein. For example, a range of “less than 10” can include any and allsub-ranges between (and including) the minimum value of zero and themaximum value of 10, that is, any and all sub-ranges having a minimumvalue of equal to or greater than zero and a maximum value of equal toor less than 10, e.g., 1 to 5. In certain cases, the numerical values asstated for the parameter can take on negative values. In this case, theexample value of range stated as “less that 10” can assume negativevalues, e.g. −1, −2, −3, −10, −20, −30, etc.

As used herein, the terms “hydrophobic” and “hydrophobicity” refer tothe wettability of a surface (e.g., a coating surface) that has a watercontact angle of approximately 85° or more. The terms “superhydrophobic”and “superhydrophobicity” refer to the wettability of a surface (e.g., acoating surface) that has a water contact angle of approximately 150° ormore and very low contact angle hysteresis (Δθ=θ_(A)−θ_(B)<1).Typically, on a hydrophobic surface, for example, a 2-mm-diameter waterdrop beads up but does not run off the surface when the surface istilted moderately. As the surface is tilted, the wetting angle at thedownhill side of the droplet increases, while the wetting angle at theuphill side of the droplet decreases. Since it is difficult for theadvancing (downhill) interface to push forward onto the next incrementof solid surface and it is difficult for the receding (uphill) interfaceto let go of its bit of solid surface, the droplet tends to remainstationary or pinned in place. A hydrophobic surface is described ashaving a low contact angle hysteresis if the difference betweenadvancing and receding contact angles is less than 1°.

In accordance with various embodiments of the present teachings, FIG. 1shows an exemplary method 100 for preparing a polymer-aerogel compositecoating, for example, an exemplary polymer-aerogel composite coating 210is shown in FIG. 2. The method 100 can include a step 101 of providing asuperhydrophobic coating solution. The superhydrophobic coating solutioncan include a surface derivatized polysilicate aerogel dispersed in afirst solvent, the polysilicate aerogel including a three dimensionalnetwork of silica particles having surface functional groups derivatizedwith a silylating agent.

In various embodiments, the step 101 of providing a superhydrophobiccoating solution can include providing an ultra high water content acidcatalyzed polysilicate aerogel formed using a third solvent, at leastone alkoxy silane precursor, water, and an acid, wherein thepolysilicate aerogel can include a three dimensional network of silicaparticles having surface functional groups and a plurality of pores. Invarious embodiments, a fluid can be disposed in the plurality of pores.Exemplary fluid can include, but is not limited to, first solvent, oneor more reaction products of the acid catalyzed hydrolysis of the alkoxysilane, and un-reacted materials such as, for example, alkoxy silaneprecursor.

In various embodiments, the alkoxy silane precursor can be organicallymodified silane monomers having a general formula of, for example,(R′)_(x)Si(OR)_(4-x), wherein x is 1 or 2 and R and R′ can be the sameor different and can include an organic group, such as, for example, analkyl, an alkenyl, an alkynyl, an aryl group, or combinations thereof.The alkoxy silane precursor can include one or more silane compoundsincluding, but not limited to, methyltrimethoxy silane, vinyltrimethoxysilane, dimethyldiethoxy silane, methacryloxypropyltrimethoxy silane,mercaptopropyltrimethoxy silane, chloropropyltrimethoxy silane,bromopropyitrimethoxy silane, iodopropyitrimethoxy silane, andchloromethyltrimethoxy silane, tetraethoxysilane, tetramethoxysilane,and 1,2-bis(triethoxysilyl) ethane. In some embodiments, the thirdsolvent can be any suitable liquid such as, for example, methanol,ethanol, and any organic solvent at least partially miscible with water.In other embodiments, the acid can be any suitable acid such as, forexample, 1.0 N hydrochloric acid and any source of hydrogen ions.

In certain embodiments, the ultra high water content acid catalyzedpolysilicate aerogel can be formed using a third solvent, at least onealkoxy silane precursor, water, and an acid, such that a molar ratio ofwater to alkoxy silane precursor can be in the range of about 10 toabout 80, which leads to the distinction of ‘ultra high water’ content.In some embodiments the molar ratio of water to alkoxy silane precursorcan be greater than about 80. In various embodiments, the polysilicateaerogel can be formed by first adding the third solvent to the alkoxysilane precursor, followed by the addition of water and the acid to forma reaction mixture. The reaction mixture can then be agitated and placedat a temperature in the range of about 15° C. to about 80° C. for aperiod of approximately 1 day to approximately 90 days, and in somecases by placing the reaction mixture at a temperature in the range ofabout 40° C. to about 60° C. for a period of approximately 3 days toapproximately 10 days. Upon the completion of the reaction, thepolysilicate aerogel can be rather firm and can have appearance fromtransparent to opaque depending upon the third solvent used. Thepolysilicate aerogel should not be loose at this stage; tapping thebottom of the reaction vessel should result in a reverberationthroughout the polysilicate aerogel. Excess water and higher levels ofacid catalyst can render the hydrolysis portion of the synthesis thedominating process and limiting the condensation. U.S. PatentApplication Publication No. 20080113188 and Master's thesis of David J.Kissel entitled, “Mechanical property characterization of sol-gelderived nanomaterials using an acoustic wave technique”, May 2007,describe in detail the sol-gel method of forming a silica gel, thedisclosures of which are incorporated by reference herein in theirentirety.

The step 101 of providing a superhydrophobic coating solution can alsoinclude replacing the fluid disposed in the plurality of pores of thepolysilicate aerogel with a fourth solvent. In various embodiments, thepolysilicate aerogel can be broken up to form a broken gel before addinga second solvent to the broken gel. Any suitable solvent immiscible withthe third solvent can be used as the fourth solvent, such as, forexample, hexane. The broken gel in the fourth solvent can be kept at atemperature in the range of about 40° C. to about 60° C. for at leastabout 30 minutes to allow solvent exchange. And finally excess of thefourth solvent and the fluid can be removed from the broken gel. Thesesteps can be repeated at least once, preferably thrice to allowreplacement of most of the fluid disposed in the plurality of pores ofthe polysilicate aerogel. Fresh fourth solvent can be added to thepolysilicate aerogel before storing in a cold storage at a temperatureof less than about 10° C. However, the polysilicate aerogel can also bestored in fresh fourth solvent at room temperature, because in somecases, the polysilicate aerogel can have a long shelf life at roomtemperature.

The step 101 of providing a superhydrophobic coating solution canfurther include derivatizing the surface functional groups of thepolysilicate aerogel using one or more silylating agents to form asurface derivatized polysilicate aerogel. In various embodiments, thederivatization of the surface functional groups of the polysilicateaerogel can include gradually adding a silylating agent adding to thepolysilicate aerogel due to silylation reaction being exothermic innature. Any suitable silane can be used as the silylating agent, suchas, for example, trimethylchlorosilane, trichloromethylsilane,trichlorooctylsilane, hexamethyldisilazane, and any reactive silaneincluding at least one hydrophobic ligand. Silylation reaction mayresult in bubbling of the solvent and once the bubbling stops, thepolysilicate aerogel can be stored in the silylating agent at atemperature in the range of about 40° C. to about 60° C. for about 6hours to about 10 hours to form a surface derivatized polysilicateaerogel and an excess of the silylating agent can be removed. While notintending to be bound by any specific theory, it is believed that thesecond solvent helps in the transport of the silylating agent forreaction with the surface functional groups, such as, for example,surface hydroxyl moieties of the polysilicate aerogel.

The step 101 of providing a superhydrophobic coating solution can alsoinclude forming a coating solution of the surface derivatizedpolysilicate aerogel in the first solvent. In various embodiments, thecoating solution of the surface derivatized polysilicate aerogelgel inthe first solvent can be formed by first washing the surface derivatizedpolysilicate aerogel with an excess of fourth solvent and washing thesurface derivatized polysilicate aerogelgel with the first solvent atleast twice before adding the first solvent to the surface derivatizedpolysilicate aerogel to form a coating solution. In certain embodiments,the surface derivatized polysilicate aerogel can be sonicated to breakup aggregates and redispersed the surface derivatized polysilicateaerogel in the first solvent. Any suitable first solvent can be used,such as, for example, ethanol. In some embodiments, the first solventcan be the same as the third solvent. In other the first solvent can bedifferent from the third solvent. In various embodiments, the surfacederivatized polysilicate aerogel in the superhydrophobic coatingsolution can have a concentration in the range of about 0.1 wt. % toabout 30 wt. % and in other cases from about 0.5 wt. % to about 10 wt.%. In some embodiments, the first solvent can be the same as the thirdsolvent.

Referring back to FIG. 1, the method 100 for preparing a polymer-aerogelcomposite coating can also include a step 102 of adding a polymersolution to the superhydrophobic coating solution to form apolymer-aerogel blend solution, wherein the polymer solution can includeone or more polymers dispersed in a second solvent. Any suitable polymercan be used in the formation of the polymer-aerogel blend solution thatcan bond with the aerogel matrix and provide structural reinforcement.Exemplary polymer can be any suitable copolymer, homopolymer, or polymerblend of one or more polymers, including, but not limited to,poly(methyl methacrylate), polystyrene, poly(butyl methacrylate),poly(tert-butyl methacrylate), poly(methyl acrylate), poly(butylacrylate), poly(tert-butyl acrylate), poly(perfluorooctyl methacrylate),and any suitable vinyl polymer. Any suitable second solvent can be usedto dissolve the polymer, such as, for example, toluene, acetone, xylene,and ethyl acetate. In some cases the second solvent can be a system ofsolvents rather than a single solvent. The polymer in the polymersolution can have any suitable concentration depending upon variousfactors, including, but not limited to, polymer type, molecular weightof the polymer, molecular weight distribution of the polymer, etc. Insome cases, the polymer in the polymer solution can have a concentrationin the range of about 1 wt. % to greater than about 50 wt. % and inother cases from about 5 wt. % to about 50 wt. %. In variousembodiments, the superhydrophobic coating can be present in a majoramount and the polymer solution can be present in a minor amount,wherein the major amount refers to volume fraction of more than about0.5 by and minor amount refers to volume fraction of less than about0.5. In some cases, the polymer solution can be added to thesuperhydrophobic coating solution at a volume fraction of about 0.05 toabout 0.25 and in other cases about 0.1 to about 0.15. However, thepolymer solution can be added to the superhydrophobic coating solutionin any desired amount.

The method 100 for preparing a polymer-aerogel composite coating canalso include a step 103 of dissolving the polymer in the polymer-aerogelblend solution at a first temperature and a step 104 of forming apolymer-aerogel composite coating by applying the polymer-aerogel blendsolution to a substrate surface while keeping the polymer-aerogel blendsolution at the first temperature or at a temperature greater than thefirst temperature, such that the polymer wets the aerogel in thepolymer-aerogel composite coating. In some embodiments, the step ofdissolving the polymer in the polymer-aerogel blend solution at a firsttemperature can include heating the polymer-aerogel blend solution alongwith stirring at a first temperature until the polymer dissolves. Insome embodiments, the first temperature can be at least about 100° C.,in other cases at least about 50° C., and in some other cases can be atleast about room temperature. In various embodiments, thepolymer-aerogel blend solution can be applied to the substrate surfaceusing any suitable technique, such as, for example, dip coating, brushcoating, roller coating, spray coating, spin coating, casting, and flowcoating. Any suitable material can be used for the substrate surface,such as, for example, metal, silicon wafers, glass, ceramics, plastics,and fabrics. In some embodiments, the step 104 of forming apolymer-aerogel composite coating can further include heating thesubstrate to a second temperature greater than the first temperature. Incertain embodiments, the second temperature can be in the range of about50° C. to about 300° C. and in some cases about 100° C. to about 250° C.However, in some embodiments, heating the substrate at the secondtemperature may not be necessary if the polymer component is welldispersed and wets in the aerogel matrix. Furthermore, heating to thesecond temperature depends on a variety of factors, including, but notlimited to, second solvent, polymer, polymer content, etc.

While not intending to be bound by any specific theory, it is believedthat during the processing of the polymer-aerogel blend solution, thepolymer and the surface derivatized polysilicate aerogel are blendedtogether to produce a phase separation prior to heating. Heating in therange of about 50° C. to about 300° C. causes the polymer to coat/wetthe surface derivatized polysilicate aerogel. Furthermore, the fact thatthe roughness of the surface derivatized polysilicate aerogel ispreserved during the deposition allows the retention of thesuperhydrophobicity of the surface derivatized polysilicate aerogel.Having too much polymer can cause the water contact angle to approachthat of the polymer itself.

FIG. 2 schematically illustrates a cross section of a portion of anexemplary article 200, in accordance with various embodiments of thepresent teachings. The exemplary article 200 can include a surface 220,the surface 220 including at least one region 230 and a polymer-aerogelcomposite coating 210 disposed over the at least one region 230, whereinthe polymer-aerogel composite coating 210 can have a water contact angleof at least about 140° and a contact angle hysteresis of less than about1°. Any suitable material can be used for the at least one region 230 ofthe surface 220, including, but not limited to, a metal, a siliconwafer, a glass, a ceramic, a plastic, and a fabric. In variousembodiments, the polymer-aerogel composite coating 220 can include oneor more polymers and an ultra high water content acid catalyzedpolysilicate gel, wherein the polysilicate aerogel can include a threedimensional network of silica particles having surface functional groupsderivatized with a silylating agent and a plurality of pores. Anysuitable polymer that can bond with the aerogel matrix and providestructural reinforcement can be used in the polymer-aerogel compositecoating 210. Exemplary polymer can be any suitable copolymer,homopolymer, or polymer blend of one or more polymers, including, butnot limited to, poly(methyl methacrylate), polystyrene, poly(butylmethacrylate), poly(tert-butyl methacrylate), poly(methyl acrylate),poly(butyl acrylate), poly(tert-butyl acrylate), poly(perfluorooctylmethacrylate), or any suitable vinyl polymer. Exemplary silylating agentcan include, but are not limited to, trimethylchlorosilane,trichloromethylsilane, trichlorooctylsilane, hexamethyldisilazane, orany reactive silane including at least one hydrophobic ligand. Thepolymer-aerogel composite coating 210 can include one or more polymersin any suitable amount. In some cases, the polymer can be present in thepolymer-aerogel composite coating in an amount from about 5% by volumeto about 50% by volume. However, the polymer can be present in thepolymer-aerogel composite coating in any suitable amount that can stillpreserve the functional surface roughness of the aerogel component ofthe polymer-aerogel composite. In various embodiments, thepolymer-aerogel composite coating 210 can have a thickness from about0.2 μm to about 3 μm. In various embodiments, the exemplarypolymer-aerogel composite coating 210 as disclosed herein can have a lowrefractive index in the range of about 1.0 to about 1.2 at about 600 nmand can be optically transparent.

In certain embodiments, the polymer-aerogel composite coating 210 canresist corrosion for about 1800 hours or longer. In various embodiments,the exemplary article 200 can include, but is not limited to an antenna,a window, an automobile, an aircraft, a building, a textile, a boat, apartially and/or fully submerged structure in water and thepolymer-aerogel composite coating 210 can be used for a wide variety ofapplications, including, but not limited to, self-cleaning surface,anti-reflective coating, anti-icing coating, a defogging coating, ananti-microbial coating, a stain resistant coating, and a drag reductioncoating in water environment. In some embodiments, the disclosedpolymer-aerogel composite coating 210 can be applied on the wings ofaircraft for the prevention of ice buildup.

In general, the polymer-aerogel composite coating 210 as disclosedherein offer all the benefits of other superhydrophobic materials, butprovides far more durability, including abrasion resistance thanconventional aerogels. Furthermore, the polymer-aerogel compositecoatings 210 of the present disclosure are less costly and are safe forbiological applications. Also, by not utilizing fluoro-alkyl silanes andsimilar fluorinated reagents in the manufacture of the polymer-aerogelcomposite coating 210, of the present disclosure, the polymer-aerogelcomposite coating 210 and the methods 100 of making them areenvironmentally friendly.

Examples are set forth herein below and are illustrative of differentamounts and types of reactants and reaction conditions that can beutilized in practicing the disclosure. It will be apparent, however,that the disclosure can be practiced with other amounts and types ofreactants and reaction conditions than those used in the examples, andthe resulting devices various different properties and uses inaccordance with the disclosure above and as pointed out hereinafter.

EXAMPLES Example 1 Preparation of Polymeric Component, Poly(MethylMethacrylate) for the Polymer-Aerogel Composite

The polymer, poly(methyl methacrylate) was prepared in about 25 mlscintillation vial without a cap. Methyl methacrylate was polymerizedthermally using azobisisobutyronitrile (AIBN) as an initiator anddodecanethiol as a chain transfer agent to skew the resulting molecularweight distribution. The weight fractions of the reagents used toprepare the polymer are given in Table 1.

TABLE 1 Material Name weight fraction Methyl methacrylate 0.982800Azobisisobutyronitrile (AIBN) 0.009828 Dodecanethiol 0.007371

After thorough mixing of the regents, the solution was set on a hotplate at a temperature of about 170° C. For UV-curing, roughly the sameweight fraction of photoinitiator was used and out gassing followed bynitrogen purging was done. After polymerization, the polymer wasdissolved in toluene followed by filtration and precipitation in ethanolfor removal of residual monomer. After removing ethanol, the polymer wasdissolved again in toluene at about 10 weight %. This solution was thenadded to the superhydrophobic coating solution to produce the compositematerial.

Example 2 Formation of Superhydrophobic Coating Solution

TABLE 2 Material Name vol. fraction for 100 mL gel volume Methanol0.0832 vol/vol 8.32 mL Tetramethylorthosilicate 0.0989 vol/vol 9.89 mL(TMOS) Dionized Water 0.8155 vol/vol 81.55 mL  1.0N Hydrochloric Acid(HCl) 0.0024 vol/vol 0.24 mL

Combined the reagents given in Table 2 according to the order in whichthey are listed. Agitated the reaction mixture and placed at about 50°C. for a period of approximately 120 hours. Upon the completion of thereaction, a gel was formed. The gel had an opaque appearance and wasrather firm. Broke up the gel with a clean utensil (e.g. stir rod,spatula, etc.) and added approximately 100 ml of hexane to the brokengel in the reaction vessel. Allowed solvent exchange for at least 30minutes at about 50° C. After solvent exchange period, removed excesshexane with a glass pipet and/or syringe and repeated the hexane wash atleast once more. After draining excess hexane, the gel was placed in acold storage in fresh hexane. Added approximately 50 ml oftrimethylchlorosilane (TMCS) (also referred to as chlorotrimethylsilane)in about 8 ml to about 12 ml increments to the gel gradually due to thereaction's exothermic nature. As soon as the bubbling stopped, thereaction vessel was closed and placed at about 50° C. for at least about8 hours. Removed the excess TMCS with a glass pipet and washed withexcess hexane (approximately 100 ml). Repeated the hexane washing atleast once more. After removal of the excess hexane, washed with excessethanol (approximately 100 ml) as was done with hexane and repeated theethanol wash at least once prior to the solution preparation. Removedexcess ethanol from the last washing step and added ethanol at a volumeappropriate for the desired thickness of the superhydrophobic coating.

Example 3 Preparation of Polymer-Aerogel Composite Coating

In an about 25 ml scintillation vial, added the superhydrophobic coatingsolution of Example 2 at a volume fraction of about 0.8696. Added thepolymer/toluene solution of Example 1 at a volume fraction of about0.1304 to the superhydrophobic coating solution of Example 2 to form apolymer-aerogel blend solution. Heated the polymer-aerogel blendsolution to about 50° C. and agitated until the polymer was dissolved.Applied the polymer-aerogel blend solution to a substrate surface whilekeeping the polymer-aerogel blend solution 50° C. to ensure properdispersion of the polymer within the aerogel matrix. After coating, thesubstrate was heated at a temperature in the range of about 180° C. toabout 200° C. for at least about 2 minutes to form a polymer-aerogelcomposite film having a thickness of about 144 nm. The as ispolymer-aerogel composite film showed a water contact angle of about159.40° and 159.30°. After destructive wearing testing, thepolymer-aerogel composite film showed a water contact angle of about143.00° and 142.50°. The destructive wearing testing was done byvigorously rubbing the polymer-aerogel composite film with a fingercovered by a rubber glove. Thus, the polymer-aerogel composite filmshowed abrasion resistance.

While the invention has been illustrated respect to one or moreimplementations, alterations and/or modifications can be made to theillustrated examples without departing from the spirit and scope of theappended claims. In addition, while a particular feature of theinvention may have been disclosed with respect to only one of severalimplementations, such feature may be combined with one or more otherfeatures of the other implementations as may be desired and advantageousfor any given or particular function. Furthermore, to the extent thatthe terms “including”, “includes”, “having”, “has”, “with”, or variantsthereof are used in either the detailed description and the claims, suchterms are intended to be inclusive in a manner similar to the term“comprising.” As used herein, the phrase “one or more of”, for example,A, B, and C means any of the following: either A, B, or C alone; orcombinations of two, such as A and B, B and C, and A and C; orcombinations of three A, B and C.

Other embodiments of the invention will be apparent to those skilled inthe art from consideration of the specification and practice of theinvention disclosed herein. It is intended that the specification andexamples be considered as exemplary only, with a true scope and spiritof the invention being indicated by the following claims.

What is claimed is:
 1. An article comprising: a surface, wherein thesurface comprises at least one region; and a polymer-aerogel compositecoating disposed over the at least one region, wherein thepolymer-aerogel composite coating comprises one or more polymers and anultra high water content catalyzed polysilicate aerogel, thepolysilicate aerogel comprising a three dimensional network of silicaparticles having surface functional groups derivatized with a silylatingagent and a plurality of pores, wherein the polymer-aerogel compositecoating has a water contact angle of at least about 140° and a contactangle hysteresis of less than about 1°.
 2. The article of claim 1,wherein the silylating agent comprises one or more oftrimethylchlorosilane, trichloromethylsilane, trichlorooctylsilane,hexamethyldisilazane, and any reactive silane including at least onehydrophobic ligand.
 3. The article of claim 1, wherein the polymercomprises one or more of poly(methyl methacrylate), polystyrene,poly(butyl methacrylate), poly(tert-butyl methacrylate), poly(methylacrylate), poly(butyl acrylate), poly(tert-butyl acrylate),poly(perfluorooctyl methacrylate), and any suitable vinyl polymer. 4.The article of claim 1, wherein the surface comprises at least one of ametal, a silicon wafer, a glass, a ceramic, a plastic, and a fabric. 5.The article of claim 1, wherein the polymer can be present in thepolymer-aerogel composite coating in an amount from about 5% by volumeto about 50% by volume.
 6. The article of claim 1, wherein thepolymer-aerogel composite coating resists corrosion for about 1800 hoursor longer.
 7. The article of claim 1, wherein the polymer-aerogelcomposite coating is used for at least one of self-cleaning surface,anti-reflective coating, anti-icing coating, a defogging coating, ananti-microbial coating, a stain resistant coating, and a drag reductioncoating in water environment.
 8. The article of claim 1, wherein thedevice comprises at least one of an antenna, a window, an automobile, anaircraft, a building, a textile, a boat, a partially and/or fullysubmerged structure in water.